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Name Reactions

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Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Alder ene reaction
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    Chapter 2 Aldol condensation
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    Chapter 3 Algar— Flynn— Oyamada Reaction
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    Chapter 4 Allan–Robinson reaction
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    Chapter 5 Arndt—Eistert homologation
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    Chapter 6 Baeyer–Villiger oxidation
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    Chapter 8 Bamford–Stevens reaction
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    Chapter 9 Barbier coupling reaction
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    Chapter 10 Bartoli indole synthesis
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    Chapter 12 Barton–McCombie deoxygenation
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    Chapter 13 Barton nitrite photolysis
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    Chapter 14 Batcho–Leimgruber indole synthesis
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    Chapter 15 Baylis–Hillman reaction
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    Chapter 16 Beckmann rearrangement
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    Chapter 17 Benzilic acid rearrangement
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    Chapter 18 Benzoin condensation
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    Chapter 19 Bergman cyclization
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    Chapter 20 Biginelli pyrimidone synthesis
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    Chapter 21 Birch reduction
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    Chapter 22 Bischler–Möhlau indole synthesis
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    Chapter 23 Bischler–Napieralski reaction
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    Chapter 24 Blaise reaction
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    Chapter 25 Blum–Ittah aziridine synthesis
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    Chapter 26 Boekelheide reaction
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    Chapter 27 Boger pyridine synthesis
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    Chapter 29 Borsche–Drechsel cyclizations
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    Chapter 30 Boulton–Katritzky rearrangement
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    Chapter 31 Bouveault aldehyde synthesis
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    Chapter 32 Bouveault—Blanc reduction
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    Chapter 33 Bradsher reaction
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    Chapter 34 Brook rearrangement
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    Chapter 35 Brown hydroboration
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    Chapter 37 Bucherer reaction
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    Chapter 38 Bucherer—Bergs reaction
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    Chapter 39 Büchner ring expansion
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    Chapter 40 Buchwald–Hartwig amination
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    Chapter 41 Burgess reagent
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    Chapter 42 Burke boronates
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    Chapter 43 Cadiot–Chodkiewicz coupling
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    Chapter 44 Camps quinoline synthesis
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    Chapter 45 Cannizzaro reaction
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    Chapter 46 Carroll rearrangement
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    Chapter 47 Castro–Stephens coupling
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    Chapter 48 Chan alkyne reduction
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    Chapter 50 Chapman rearrangement
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    Chapter 51 Chichibabin pyridine synthesis
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    Chapter 52 Chugaev elimination
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    Chapter 53 Ciamician–Dennsted rearrangement
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    Chapter 54 Claisen condensation
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    Chapter 55 Claisen isoxazole synthesis
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    Chapter 57 Clemmensen reduction
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    Chapter 58 Combes quinoline synthesis
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    Chapter 59 Conrad–Limpach reaction
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    Chapter 60 Cope elimination reaction
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    Chapter 62 Corey–Bakshi–Shibata (CBS) reagent
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    Chapter 63 Corey–Chaykovsky reaction
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    Chapter 64 Corey–Fuchs reaction
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    Chapter 65 Corey–Kim oxidation
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    Chapter 66 Corey–Nicolaou macrolactonization
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    Chapter 67 Corey–Seebach reaction
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    Chapter 68 Corey–Winter olefin synthesis
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    Chapter 69 Criegee glycol cleavage
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    Chapter 70 Criegee mechanism of ozonolysis
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    Chapter 71 Curtius rearrangement
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    Chapter 72 Dakin oxidation
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    Chapter 73 Dakin–West reaction
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    Chapter 74 Darzens condensation
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    Chapter 75 Delépine amine synthesis
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    Chapter 76 de Mayo reaction
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    Chapter 77 Demjanov rearrangement
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    Chapter 79 Dieckmann condensation
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    Chapter 81 Dienone–phenol rearrangement
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    Chapter 82 Di–π–methane rearrangement
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    Chapter 83 Doebner quinoline synthesis
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    Chapter 84 Doebner–von Miller reaction
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    Chapter 85 Dötz reaction
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    Chapter 86 Dowd–Beckwith ring expansion
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    Chapter 87 Dudley reagent
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    Chapter 88 Erlenmeyer–Plöchl azlactone synthesis
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    Chapter 89 Eschenmoser’s salt
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    Chapter 91 Eschweiler–Clarke reductive alkylation of amines
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    Chapter 92 Evans aldol reaction
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    Chapter 94 Feist–Bénary furan synthesis
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    Chapter 96 Ferrier glycal allylic rearrangement
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    Chapter 97 Fiesselmann thiophene synthesis
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    Chapter 98 Fischer indole synthesis
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    Chapter 99 Fischer oxazole synthesis
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    Chapter 100 Fleming–Kumada oxidation
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    Chapter 102 Friedländer quinoline synthesis
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    Chapter 103 Fries rearrangement
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    Chapter 104 Fukuyama amine synthesis
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    Chapter 105 Fukuyama reduction
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    Chapter 106 Gabriel synthesis
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    Chapter 107 Gabriel–Colman rearrangement
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    Chapter 108 Gassman indole synthesis
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    Chapter 109 Gattermann–Koch reaction
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    Chapter 110 Gewald aminothiophene synthesis
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    Chapter 112 Gomberg–Bachmann reaction
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    Chapter 113 Name Reactions
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    Chapter 114 Grignard reaction
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    Chapter 115 Grob fragmentation
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    Chapter 116 Guareschi–Thorpe condensation
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    Chapter 117 Hajos–Wiechert reaction
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    Chapter 118 Haller–Bauer reaction
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    Chapter 119 Hantzsch dihydropyridine synthesis
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    Chapter 120 Hantzsch pyrrole synthesis
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    Chapter 122 Hegedus indole synthesis
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    Chapter 123 Hell—Volhard—Zelinsky reaction
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    Chapter 124 Henry nitroaldol reaction
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    Chapter 125 Hinsberg synthesis of thiophene derivatives
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    Chapter 126 Hiyama cross-coupling reaction
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    Chapter 127 Hofmann rearrangement
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    Chapter 128 Hofmann–Löffler–Freytag reaction
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    Chapter 129 Horner—Wadsworth—Emmons reaction
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    Chapter 130 Houben–Hoesch reaction
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    Chapter 131 Hunsdiecker–Borodin reaction
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    Chapter 132 Jacobsen–Katsuki epoxidation
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    Chapter 133 Japp–Klingemann hydrazone synthesis
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    Chapter 135 Julia–Kocienski olefination
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    Chapter 136 Julia–Lythgoe olefination
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    Chapter 138 Knoevenagel condensation
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    Chapter 139 Knorr pyrazole synthesis
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    Chapter 140 Koch–Haaf carbonylation
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    Chapter 141 Koenig–Knorr glycosidation
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    Chapter 142 Kostanecki reaction
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    Chapter 143 Kröhnke pyridine synthesis
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    Chapter 144 Kumada cross-coupling reaction
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    Chapter 145 Lawesson’s reagent
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    Chapter 146 Leuckart–Wallach reaction
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    Chapter 147 Lossen rearrangement
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    Chapter 148 McFadyen–Stevens reduction
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    Chapter 149 McMurry coupling
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    Chapter 150 Mannich reaction
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    Chapter 151 Martin’s sulfurane dehydrating reagent
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    Chapter 152 Masamune–Roush conditions for the Horner–Emmons reaction
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    Chapter 154 Meerwein–Ponndorf–Verley reduction
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    Chapter 155 Meisenheimer complex
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    Chapter 156 [1,2]-Meisenheimer rearrangement
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    Chapter 157 [2,3]-Meisenheimer rearrangement
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    Chapter 158 Meyers oxazoline method
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    Chapter 159 Meyer–Schuster rearrangement
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    Chapter 160 Michael addition
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    Chapter 161 Michaelis–Arbuzov phosphonate synthesis
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    Chapter 162 Midland reduction
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    Chapter 163 Minisci reaction
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    Chapter 164 Mislow–Evans rearrangement
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    Chapter 165 Mitsunobu reaction
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    Chapter 166 Miyaura borylation
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    Chapter 167 Moffatt oxidation
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    Chapter 168 Morgan–Walls reaction
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    Chapter 169 Mori–Ban indole synthesis
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    Chapter 170 Mukaiyama aldol reaction
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    Chapter 171 Mukaiyama Michael addition
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    Chapter 172 Mukaiyama reagent
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    Chapter 173 Myers–Saito cyclization
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    Chapter 174 Nazarov cyclization
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    Chapter 175 Neber rearrangement
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    Chapter 176 Nef reaction
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    Chapter 177 Negishi cross-coupling reaction
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    Chapter 178 Nenitzescu indole synthesis
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    Chapter 179 Newman–Kwart rearrangement
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    Chapter 180 Nicholas reaction
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    Chapter 181 Nicolaou IBX dehydrogenation
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    Chapter 182 Noyori asymmetric hydrogenation
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    Chapter 183 Nozaki–Hiyama–Kishi reaction
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    Chapter 184 Nysted reagent
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    Chapter 185 Oppenauer oxidation
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    Chapter 186 Overman rearrangement
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    Chapter 187 Paal thiophene synthesis
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    Chapter 188 Paal–Knorr furan synthesis
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    Chapter 189 Paal–Knorr pyrrole synthesis
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    Chapter 190 Parham cyclization
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    Chapter 191 Passerini reaction
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    Chapter 192 Paternó–Büchi reaction
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    Chapter 193 Pauson–Khand reaction
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    Chapter 194 Payne rearrangement
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    Chapter 195 Pechmann coumarin synthesis
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    Chapter 196 Perkin reaction
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    Chapter 197 Petasis reaction
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    Chapter 198 Petasis reagent
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    Chapter 199 Peterson olefination
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    Chapter 200 Pictet–Gams isoquinoline synthesis
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    Chapter 201 Pictet–Spengler tetrahydroisoquinoline synthesis
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    Chapter 202 Pinacol rearrangement
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    Chapter 203 Pinner reaction
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    Chapter 204 Polonovski reaction
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    Chapter 205 Polonovski–Potier reaction
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    Chapter 206 Pomeranz–Fritsch reaction
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    Chapter 207 Prévost trans-dihydroxylation
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    Chapter 208 Prins reaction
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    Chapter 209 Pschorr cyclization
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    Chapter 210 Pummerer rearrangement
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    Chapter 211 Ramberg–Bäcklund reaction
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    Chapter 212 Reformatsky reaction
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    Chapter 213 Regitz diazo synthesis
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    Chapter 214 Reimer–Tiemann reaction
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    Chapter 215 Reissert reaction
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    Chapter 216 Reissert indole synthesis
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    Chapter 217 Ring-closing metathesis (RCM)
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    Chapter 218 Ritter reaction
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    Chapter 219 Robinson annulation
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    Chapter 220 Robinson–Gabriel synthesis
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    Chapter 221 Robinson–Schöpf reaction
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    Chapter 222 Rosenmund reduction
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    Chapter 223 Rubottom oxidation
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    Chapter 224 Rupe rearrangement
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    Chapter 225 Saegusa oxidation
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    Chapter 226 Sakurai allylation reaction
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    Chapter 227 Sandmeyer reaction
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    Chapter 228 Schiemann reaction
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    Chapter 229 Schmidt rearrangement
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    Chapter 230 Schmidt’s trichloroacetimidate glycosidation reaction
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    Chapter 231 Shapiro reaction
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    Chapter 232 Sharpless asymmetric amino-hydroxylation
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    Chapter 233 Sharpless asymmetric dihydroxylation
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    Chapter 234 Sharpless asymmetric epoxidation
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    Chapter 235 Sharpless olefin synthesis
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    Chapter 236 Simmons–Smith reaction
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    Chapter 237 Skraup quinoline synthesis
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    Chapter 239 Sommelet reaction
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    Chapter 240 Sommelet–Hauser rearrangement
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    Chapter 241 Sonogashira reaction
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    Chapter 242 Staudinger ketene cycloaddition
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    Chapter 243 Staudinger reduction
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    Chapter 244 Stetter reaction
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    Chapter 245 Still–Gennari phosphonate reaction
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    Chapter 246 Stille coupling
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    Chapter 247 Stille–Kelly reaction
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    Chapter 248 Stobbe condensation
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    Chapter 249 Strecker amino acid synthesis
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    Chapter 250 Suzuki–Miyaura coupling
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    Chapter 251 Swern oxidation
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    Chapter 252 Takai reaction
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    Chapter 253 Tebbe’s reagent
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    Chapter 254 TEMPO oxidation
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    Chapter 256 Tsuji–Trost reaction
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    Chapter 257 Ugi reaction
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    Chapter 258 Ullmann coupling
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    Chapter 259 van Leusen oxazole synthesis
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    Chapter 260 Vilsmeier– Haack reaction
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    Chapter 261 Vinylcyclopropane–cyclopentene rearrangement
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    Chapter 262 von Braun reaction
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    Chapter 263 Wacker oxidation
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    Chapter 264 Wagner–Meerwein rearrangement
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    Chapter 265 Weiss–Cook reaction
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    Chapter 266 Wharton reaction
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    Chapter 267 White Reagent
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    Chapter 268 Willgerodt–Kindler reaction
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    Chapter 270 [1,2]-Wittig rearrangement
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    Chapter 271 [2,3]-Wittig rearrangement
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    Chapter 272 Wohl–Ziegler reaction
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    Chapter 273 Wolff rearrangement
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    Chapter 274 Wolff–Kishner reduction
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    Chapter 275 Woodward cis-dihydroxylation
  256. Altmetric Badge
    Chapter 276 Yamaguchi esterification
  257. Altmetric Badge
    Chapter 277 Zincke reaction
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Title
Name Reactions
Published by
Springer Berlin Heidelberg, January 2009
DOI 10.1007/978-3-642-01053-8
ISBNs
978-3-64-201052-1, 978-3-64-201053-8
Authors

Li, Jie Jack

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The data shown below were compiled from readership statistics for 140 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 <1%
Brazil 1 <1%
Unknown 138 99%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 25 18%
Student > Bachelor 21 15%
Student > Master 19 14%
Student > Doctoral Student 8 6%
Researcher 7 5%
Other 18 13%
Unknown 42 30%
Readers by discipline Count As %
Chemistry 72 51%
Pharmacology, Toxicology and Pharmaceutical Science 8 6%
Biochemistry, Genetics and Molecular Biology 4 3%
Engineering 4 3%
Neuroscience 1 <1%
Other 3 2%
Unknown 48 34%